FDAnews Announces — Protecting Your Clinical Trial Data: Complying with Foreign and Domestic Privacy Laws Webinar, Sept. 22, 2016

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More than 100 countries have passed national privacy laws applying to all types of clinical trial data. Join Joan Antokel, Managing Partner, Park Legal LLC, on Sept. 22 when she’ll discuss the key changes that impact clinical trials and the FDA’s and other regulators’ expectations for compliance.

Protecting Your Clinical Trial Data:
Complying with Foreign and Domestic Privacy Laws
**An FDAnews Webinar**
Sept. 22, 2016 — 1:30 p.m. – 3:00 p.m. ET
http://info.fdanews.com/protecting-your-clinical-trial-data-pr

More than 100 countries have passed national privacy laws applying to all types of data. From the U.S.’s HIPPA/HITECH to Europe’s GDPR, regulations influence where trials are conducted — how to collect — store — and transfer research data.

Trial sponsors need to know that the data are safe and secure from security threats.

Join Joan Antokel — Managing Partner, Park Legal LLC — on Sept. 22 when she’ll discuss the key changes that impact clinical trials and the FDA’s and other regulators’ expectations for compliance.

Attendees will learn:

  • Pros and cons of using software apps in the research context
  • Patient recruitment techniques via the web and social media
  • Secondary uses of research data
  • Data security issues for research
  • Data transfer compliance — including Privacy Shield
  • New EU General Data Protection Regulation and the impact on global clinical research

Register today and examine important data collection issues that sponsors can encounter in clinical trials.

Meet the Presenter:
Joan Antokol, Managing Partner, Park Legal LLC
Joan Antokol is internationally recognized for her work in privacy and data protection. She is the managing partner of Park Legal LLC, a new Indianapolis-based boutique law firm that focuses its practice in the areas of data privacy, information security and records management. She assists organizations with many aspects of privacy and security, including healthcare and clinical research, security breaches, international data transfers, enterprise management, and privacy auditing.

Who Will Benefit:

  • Medical Affairs Officers
  • Director of Clinical Operations
  • Regulatory Affairs Professionals
  • Director of Publications
  • Director of Clinical Trial Regulatory Management
  • Clinical Trial Information Disclosure Directors
  • Global Clinical Safety and Pharmacovigilance Officers

Webinar Details:
Protecting Your Clinical Trial Data:
Complying with Foreign and Domestic Privacy Laws
Sept. 22, 2016 — 1:30 p.m. – 3:00 p.m. ET
http://info.fdanews.com/protecting-your-clinical-trial-data-pr

Tuition:
$287 per site

Easy Ways to Register:
Online: http://info.fdanews.com/protecting-your-clinical-trial-data-pr                            
By phone: 888-838-5578 or 703-538-7600

About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations.

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Michelle Butler
FDANEWS
+1 (703) 538-7665
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